Evidence map›Paper›PMID 32921688›Full record

ArticleInternal medicine (Tokyo, Japan)2021

Celiac Disease Complicated by Rhabdomyolysis.

Mia Fujisawa, Masashi Matsushima, Takashi Ueda, Motoki Kaneko, Ryutaro Fujimoto, Masaya Sano, Erika Teramura, Makiko Monma, Hajime Mizukami, Fumio Nakahara and 2 more

Open access · diamondAbstract read
In one paragraph

Article in Internal medicine (Tokyo, Japan), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 40% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 1 institution in 1 country.

Mia FujisawaDivisions of Gastroenterology and Hepatology, Department of Internal Medicine, Tokai University, School of Medicine, Japan.
Masashi MatsushimaDivisions of Gastroenterology and Hepatology, Department of Internal Medicine, Tokai University, School of Medicine, Japan.
Takashi UedaDivisions of Gastroenterology and Hepatology, Department of Internal Medicine, Tokai University, School of Medicine, Japan.
Motoki KanekoDivisions of Gastroenterology and Hepatology, Department of Internal Medicine, Tokai University, School of Medicine, Japan.
Ryutaro FujimotoDivisions of Gastroenterology and Hepatology, Department of Internal Medicine, Tokai University, School of Medicine, Japan.
Masaya SanoDivisions of Gastroenterology and Hepatology, Department of Internal Medicine, Tokai University, School of Medicine, Japan.
Erika TeramuraDivisions of Gastroenterology and Hepatology, Department of Internal Medicine, Tokai University, School of Medicine, Japan.
Makiko MonmaDivisions of Gastroenterology and Hepatology, Department of Internal Medicine, Tokai University, School of Medicine, Japan.
Hajime MizukamiDivisions of Gastroenterology and Hepatology, Department of Internal Medicine, Tokai University, School of Medicine, Japan.
Fumio NakaharaDivisions of Gastroenterology and Hepatology, Department of Internal Medicine, Tokai University, School of Medicine, Japan.
Hidekazu SuzukiDivisions of Gastroenterology and Hepatology, Department of Internal Medicine, Tokai University, School of Medicine, Japan.
Takayoshi SuzukiDivisions of Gastroenterology and Hepatology, Department of Internal Medicine, Tokai University, School of Medicine, Japan.
Tokai University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

At 37 years old, a patient developed chronic watery diarrhea, generalized pain, severe hypokalemia and elevated creatine kinase levels. She was thought to have rhabdomyolysis due to hypokalemia from chronic diarrhea. No organic cause was found. Her symptoms subsided with potassium correction, but hypokalemia persisted; she visited our hospital at 44 years old. Endoscopy detected prominent atrophy of the intestinal villi. Histology indicated Marsh-Oberhuber type-3b disease. Anti-gliadin and anti-tissue transglutaminase IgA antibody tests were positive. She was diagnosed with celiac disease and started on a gluten-free diet, which improved her symptoms. This report is only the tenth of its kind worldwide.

Indexed as

Celiac DiseaseRhabdomyolysisAdultDuodenumFemaleGliadinHumansImmunoglobulin AIntestinal MucosaGliadinImmunoglobulin Aceliac diseasehypokalemiarhabdomyolysis

Identifiers

PMID32921688
PMCPMC7872804
OpenAlexW3086780313

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.